Stable DNA Nanomachine Based on Duplex–Triplex Transition for

May 27, 2015 - DNA nanomachines are becoming useful tools for molecular recognition, imaging, and diagnostics and have drawn gradual attention. Unfort...
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A Stable DNA Nanomachine Based on Duplex-triplex Transition for Ratiometric Imaging Instantaneous pH Changes in Living Cells Mengqi Yang, Xiaoling Zhang, Haipeng Liu, Huaizhi Kang, Zhi Zhu, Wen Yang, and Weihong Tan Anal. Chem., Just Accepted Manuscript • DOI: 10.1021/acs.analchem.5b01233 • Publication Date (Web): 27 May 2015 Downloaded from http://pubs.acs.org on June 2, 2015

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Analytical Chemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

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A Stable DNA Nanomachine Based on Duplex-triplex Transition for Ratiometric Imaging Instantaneous pH Changes in Living Cells 1

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Mengqi Yanga, Xiaoling Zhanga*, Haipeng Liub, Huaizhi Kang b, Zhi Zhub, Wen Yanga* , Weihong Tanb* 15

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a. Key Laboratory of Cluster Science of Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry, Beijing Institute of Technology, 5 Zhongguancun Road, Beijing 100081, P. R. China.

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b. Center for Research at Bio/nano Interface, Department of Chemistry and Department of Physiology and Functional Genomics, Shands Cancer Center, UF Genetics Institute and McKnight Brain Institute, University of Florida, Gainesville, Florida 32611-7200, USA.

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ABSTRACT: DNA nanomachines are becoming useful tools for molecular recognition, imaging, diagnostics and have drawn gradual attention. Unfortunately, the present application of most DNA nanomachines is limited in vitro, so expanding their application in organism has becoming primary. Hence, a novel DNA nanomachine named t-switch, based on DNA duplex-triplex transition, is developed for motoring intracellular pH gradient. Our strategy is based on DNA triplex structure containing C+-G-C triplets and pH-depended FRET. Our results indicate that t-switch is an efficient reporter of pH from pH 5.3 to 6.0 with a fast response of a few seconds. And the uptake of t-switch is speedy. In order to protects t-switch from enzymatic degradation, PEI is used for modification of our DNA nanomachine. At the same time, the dynamic range could be extended to pH 4.6-7.8. The successful application of this pH-depended DNA nanomachine and motoring spatiotemporal pH changes associated with endocytosis is strong evidence of the possibility of selfassembly DNA nanomachine for imaging, targeted therapies and controllable drug delivery.

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35 DNA is an attractive and useful material for constructing functional architectures1-9. A large number of nanomachines based on DNA scaffold, such as DNA tweezer, walker and motors10-13 have been reported. Design of novel DNA nanomachines has attracted particularly attention because of their many potential applications in nanoelectronic devices, biosensors, molecular computation, and smart materials14-17. Based on different response mechanisms including conformation changes, strand displacement, and enzymatic activity, a variety of DNA structures, such as i-motif, G-quadruplex and triplex, have been used as building blocks for constructing nanomachines18-20. Each of these DNA nanomachines can respond to specific triggers and convert to an output due to the conformation changes. Owing to the specificity and biocompatibility of DNA nanomachine, it is highly interesting to fabricate DNA nanomachines into powerful biosensors that can monitor chemical stimuli in vitro and in vivo. However, applications of DNA nanomachines in vivo are difficult to

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exploit owing to the difficulty in cellular internalization of negatively charged DNA21-25. pH plays a critical role in living cells, and its biological significance has attracted much attention. Intracellular pH (pHi) changes, especially in organelles, are connected with many physiological processes such as internalization pathways26,27 and muscle contraction28,29. On the other hand, abnormal pHi values are associated with inappropriate cell function, growth, cell proliferation and apoptosis30-36. Besides, some common disease, such as cancer37 and Alzheimer's disease38, are characterized by pHi changes in biological events. As a consequence, motoring pHi gradient is highly important but remains a great challenge. Hence, many pH-sensitive DNA nanomachines and non-DNA-based pH sensors, including organic fluorescent probes, nanosensors and fluorescent proteins, have been reported to be used in vivo. But these non-DNA-based pH sensors have their certain defects. For instance, some organic fluorescent probes39-43 suffer from complicated synthesis, bad biocompatibility, poor light stability and high cytotoxicity. Nanosensors, constructed

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Analytical Chemistry from quantum dots44-45, polymers46-52, metal 53-55 nanoparticles and carbon nanomaterials56-58, are limited by low loading rate of dye, poor repeatability and controversial cytotoxicity. Likewise, fluorescent proteins5960 could only be expressed though complicated encoding, synthesis and strict experiment operating. Therefore, these drawbacks may limit their application in cellular measurements. Compared with non-DNA-based pHi sensors, pH-sensitive DNA nanomachines show certain advantages61-65. DNA is a kind of environmental friendly new material with stable physical and chemical properties. The synthetic of DNA sequence is simple, and it’s convenient to modify. At the same time, based on accurate principle of complementary base pairing, design of DNA nanomachines is predictable and programmable. In a word, DNA nanomachine is an ideal tool to detect pHi. However, although several pHdepended DNA nanomachines66-69 have been reported, most of them can only be used in vitro. At present, iswitch has been used in vivo, which is the first example of an autonomous DNA nanomachine that can respond to a specific molecular trigger in living cell70,71. Unfortunately, i-switch could only map pH changes on long timescales of a few minutes in vivo, which is unsuitable for monitoring instantaneous biological processes. Therefore, design of DNA nanomachines which can be used in vivo for catching pH changes on short time scales is a challenge but desirable task.

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Here a novel DNA nanomachine based on DNA duplextriplex transition (t-switch) is developed to monitor pHi gradient. Our approach is based on the principle of a DNA triplex nanomachine containing C+-G-C triplets. A pHdependent FRET is recorded during the duplex-triplex transition process72,73, demonstrating that t-switch is an efficient pH sensor from pH 5.3 to 6.0 and could be uptaken by cells easily. Furthermore, to facilitate endocytosis process74,75 and protects t-switch from enzymatic degradation, PEI, a common cationic polymer for gene transfer, is used for packing t-switch. Surprisingly, the dynamic responding range of t-switch can be extended to 4.6-7.8 by complexing with PEI. Moreover, t-switch could function autonomously inside living HepG2 cells to map and monitor intracellular pH changes after endocytosis.

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Scheme 1. The construction and principle of t-switch in the "open" state (low FRET) at high pH and in the "closed" state (high FRET) at low pH.

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As the working principle shown in Scheme 1, t-switch is consisted of three oligonucleotide strands A, B and C, where B and C can hybridize with A, leaving a one-base gap. Both strand A and B have overhangs at 5' termini which are labeled with pH-insensitive dye Alexa-488 and Alexa-647, respectively. The cytosine (C) riched overhang of strand A is single-stranded, while the overhang of strand B is double-stranded which contains CG bases. At high pH as the “open state” of the t-switch, these two overhangs form an extended duplex conformation to separate the two fluorophores and avoid FRET happening. However, in acidic conditions the single-stranded overhang of strand A will bind in a parallel orientation to the double-stranded overhang of strand B. Therefore, the C+-G-C triad structured will be formed to induce the triplex structure of t-switch, yielding a "closed state" to bring two fluorophores into proximity. As a result, FRET could take place between Alexa-488/647 FRET pair. Thus, the formation of the triplex and the exhibition of FRET signal could be sensitive to pH. Inspired by published work66, we design the sequences of t-switch which shown in Table S1. The fluorescence properties of t-switch are first investigated as a function of pH to determine its pH responsive range (Figure 1a). With the decrease of pH value, a gradual decrease of fluorescent intensity at 520 nm for donor fluorophore has been observed, while a new florescence peak appears at 665 nm for acceptor fluorophore. Therefore, donor fluorescence decreases while acceptor fluorescence increases as a result of FRET, indicating the transition from open to closed state of tswitch upon the pH change. The plot of fluorescence ratios (D/A) of Alexa-488/647-labelled t-switch as a function of pH (Figure 1b) shows a sigmoid increase between pH 5.3 and 6.0 with 4-fold ratio increase and the pKa value is determined to be 5.67(the calculation is shown in supporting information, Figure S2a). This makes it a well nanomachine to track fine pH changes associated with endosomal maturation.

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Analytical Chemistry

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13 Figure 1. In vitro characterization of t-switch. a) Emission responses of t-switch (80 nM) toward pH change in PBS (20 mM). Inset: pH-dependent responses of emission between 640 nm and 750 nm. b) The calibration curve of t-switch showing normalized donor/acceptor (D/A) intensity (Alexa488/Alexa-647) ratios. c) Working cycling of the t-switch. Fluorescence intensity was monitored at 520 nm by excited at 488 nm while the solution pH value oscillated between 5.0 and 8.0. d) Response time for the transition between the open and closed states. Addition of base and acid was shown by arrows.

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25 The in vivo performance of t-switch is then evaluated by incubating t-switch with cells. 80 nM t-switch is added to cultured HepG2 cells. After incubating for 10 min at 37˚C, cells are washed 3 times with PBS buffer. The confocal images are shown in Figure 2a. The uptake of t-switch by living cells is speedy, and some t-switches are distributed in lysosomes (Figure S4). In green channel, the fluorescence intensity of Alex488 is variable within single cells consistent with uneven intracellular pH distributions while fluorescence signal is very weak in red channel (Alex 647). It may be that DNA nanomachines partly be internalized through anion channels and entered into

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early endosomes which will become lysosomes after a series of physiological changes70. During this process, pH value will deceases from 7.4 inside early endosomes to 5.0 in lysosomes (Figure S5)76-79, and t-switches will be in two stages with different pH value. In early endosomes, the pH is 7.4-6.0 while C+-G-C triad structure only formed when pH blow 6.0. So t-switches are in “open” state and FRET couldn’t happen. On the other hand, when early endosomes become late endosomes and lysosomes, where pH is below 6.0, t-switches are in “close” state and signal in red channel is observed in Figure 2a. Moreover, it becomes brighter as time goes on (enlarged images of red channel are shown in Figure S6). This means a increasing number of t-switches turn to “close” state as endosomes becoming lysosomes. Besides the reason above, we think that elaborate enzyme system in lysosomes may affect the stability of t-switch. This could also lead to weak signal in red channel. Then, lactate buffer (pH 6.0) and 5-(N,Ndimethyl)amiloride (DMA), an inhibitor of Na+/H+ exchanger, are added to induce the decrease of intracellular pH80-82. Upon the treatment, the reduction of pH value induces the formation of “close” state, resulting in bright fluorescence signals in red channel (Figure 2b). At the same time, there are obvious changes of fluorescence intensity in both green channel and red channel (Figure S7). Partial enlarged ratiometric images of acidation HepG2 cells are shown in Figure S8. This pH change caused by acidizing is confirmed by using BCECFAM as a pH indicator and the result are shown in Figure S9. More confocal images of RAW264.7 cells are mentioned in supporting information (Figure S10). Although the cellular co-localization of t-switch and LysoTracker Red shows that the uptake of t-switch is speedy, we suspect that it is hard for t-switch to remain stably inside cells according to the weaker signal in red channel in Figure 2a. So how to improve it’s stability is the crux of the matter.

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53 Figure 2. Confocal fluorescence images of t-switch in live HepG2 cells. a) Imaging of t-switch in normal cells. b) Imaging of tswitch in cells after acidizing.

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channel of Figure 2a. In lysosomes, construction of some t-switches will be destroyed because of high concentration and activity of DNase II.

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9 Figure 3. In vitro characterization of the PEI/DNA complexes. a, pH-dependent emission spectra changes of PEI/DNA complex (20 nM) in PBS at 25 ˚C. b, The donor/acceptor (D/A) intensity (Alexa-488/Alexa-647) ratios changes in vitro.

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Lysosomes are important acid organelles in cells. Abnormal functions of lysosomes are associated with many diseases such as silicosis, rheumatoid arthritis (RA) and all kinds of lysosomal storage disorder. Meanwhile, the relationship of lysosomes and tumor increasingly aroused people’s concern. Therefore, monitoring pH changes between different functional phases of lysosomes is of great significance. However, there are large amount of DNase in lysosomes and posing a threat to the stability of t-switch. We think this maybe the reason why our tswitch couldn’t remain stably in cells. Therefore we explore the idea of polyplex to facilitate cell internalization of our pH-sensitive DNA nanodevice. PEI facilitates the internalization of DNA by complexing with DNA through electrostatic interactions and also protects DNA from enzymatic degradation83,84. After mixing with PEI at an N/P ratio of 1:3, DNA is efficiently condensed into particle-like complexes with sizes range from 20 to 50 nm (Figure S3b). The PEI/DNA complex did not affect the function of t-switch, as shown in Figure 3a. Surprisingly, the response pH of t-switch is extended to pH 4.6-7.8 with the pKa value of 6.53 (Figure S2b), most likely due to the pH sponge effect of PEI. The wide range is composed with two ranges: pH 4.6-5.8 and pH 5.8-7.8. Meanwhile, forming complex with PEI didn’t influence the fast response of t-switch to pH (Figure 4b).

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The stability of t-switch in living cells is very important for application in vivo. Therefore, in order to prove our conjecture, we imitate ambient of lysosomes and investigate the stability of t-switch in different conditions. As shown in Figure 5, its stability in the presence of DNase II is greatly enhanced after forming complex with PEI. Sharp decrease of fluorescence intensity appears when DNase II is added to the naked t-switch. In contrast, only slightly decrease of fluorescence is observed within 330 min for PEI/DNA complex. Taken together, the above observations show that PEI not only extends the pH working range for t-switch, but also offers protection capablity against cellular enzymes. These experimental results also prove our hypothesis on the second reason why fluorescence signal is weak in red

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Figure 4. a) Working cycling of PEI/DNA complexes. Fluorescence intensity was monitored at 520 nm by excited at 488 nm while the solution pH value oscillated between 5.0 and 8.0. b) Response time for the formation of the open and closed states. Addition of base and acid was shown by arrows.

Furthermore, HepG2 cells are incubated with the PEI/DNA complex (20 nM) for 20 min at 37˚C and then washed three times with PBS buffer. The PEI/DNA complex can enter cells by endocytosis pathway. As PEI//DNA complex in endosomes where pH value is just in it’s dynamic range, there are some hotspots in red channel (Figure 6) while bare t-switch show weaker fluorescence signal in the same field (Figure 2a). The fluorescence changes along with time could be observed via monitoring hotspots in red channel (Figure S12). Partial enlarged ratiometric images of single HepG2 cell are shown in Figure S11.

Figure 5. Experiments aimed at understanding the stability of t-switch. Fluorescence intensities at 675 nm in the presence or absence of DNase II in t-switch or PEI/DNA complexes respectively.

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Analytical Chemistry response, relative stability to enzyme and wide dynamic range. The successful application of this pH-depended DNA nanomachine and monitoring spatiotemporal pH changes associated with endocytosis could be useful for the future application of self-assembled DNA nanomachine in the field of imaging, targeted therapies and controllable drug delivery.

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7 Figure 6. Confocal fluorescence images of PEI/DNA complex in HepG2 cells.

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Confocal experiments show that t-switch could enter living HepG2 cells within 10 min while it is well known that the uptake of naked DNA is difficult. In order to explain the fast uptake, we study the cellular internalization ability of t-switch. Our t-switch and dyelabelled single-stranded DNA (strand A and strand B) are incubated with different cells, respectively. The confocal fluorescence images show that t-switch could be assimilated easily by the testing cells, while it is difficult for strand A and B to internalize. We conjecture that the presence of nanostructure is crucial for efficient cellular internalization (Figure S13). Besides, the internalization mechanism of t-switch and PEI/DNA complex is further investigated by incubating them with HepG2 cells after inhibition of endocytosis by potassium depletion85, respectively. The flow cytometric analysis results shown in Figure S14 and Figure S15 indicate that after blocking the endocytosis pathway, delivery of PEI/DNA complexes is effectively inhibited, while the uptake of naked t-switch isn’t affected. Date of the mean fluorescence intensity and the number of selected cells in different conditions are shown in Table S2. Our researches indicate that t-switch may enter living cells through other internalization pathway. More details about their routes of entry still need be investigated.

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In conclusion, we have demonstrated a FRET-based DNA nanomachine for fast-responding mapping pH changes in living cells. The as-designed t-switch is sensitive to pH between pH 5.3 to 6.0. Remarkably, it is on timescales of a few seconds while other DNA nanomachines are on long timescales of a few minutes. The fast response speed makes it easy to catch pH changes associated with instantaneous biological processes on shorter timescales. Evidently, t-switch shows excellent reversibility for several pH cycles, after repetitive addition of NaOH and HCl diluted the sample. More importantly, t-switch can gain entrance to living cells without any transfection reagent in a few minutes. For stability and inducing endocytosis, PEI is used to form PEI-DNA nanomachine complex. In addition to a wide dynamic range of pH 4.6-7.8, complexing with PEI could protect t-switch from enzyme decomposition in endosomes and lysosomes. Therefore, t-switch is expected to be used as a reporter of intracellular pH changes associated with biological processes due to its fast

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Experimental Section DNA oligonucleotides purifiedd by high-performance liquid chromatography (Strand A, B and C) are purchased from Invitrogen. UV-vis absorption spectra are obtained on a PE-Lambda 35 UV-vis spectrophotometer with a quartz cuvette (path length = 1 cm). The pH measurements are made with a Sartorius basic pH-meter PB-10. Fluorescence measurements are taken on a Hitachi F-4600 fluorescence spectrometer, samples are excited at 488 nm and emission is collected between 500 nm and 750 nm. Confocal images are taken on a confocal laser scanning biological microscope FV1000-LX81 Olympus. PEI, Ca-lactate and DNase II are purchased from J&K Scientific Ltd.. 5-(N,N-dimethyl)amiloride (DMA) is acquired from Sigma. All other reagents and chemicals used in this paper are obtained from commercial suppliers unless noted otherwise. The pH is adjusted to the desired values at room temperature with either HCl or NaOH. Lactate buffer (pH 6.0) is prepared according to published procedures80.

ASSOCIATED CONTENT Supporting Information Experimental details, Table S1-S2, and Figure S1-S15 mentioned in text is shown in supporting information. This material is available free of charge via the Internet at http://pubs.acs.org.”

AUTHOR INFORMATION Corresponding Author a*E-mail: [email protected]. E-mail:[email protected]. b*E-mali: [email protected]

Notes The authors declare no competing financial interest.

ACKNOWLEDGMENT We would like to thank Dr. Hongying Jia in Institute of Chemistry Chinese Academy of Sciences for enthusiastic help in the cytological experiments. We gratefully acknowledge financial support from the National Nature Science Foundation of China (No. 21275018 and 21203008), Beijing National Laboratory for Molecular Sciences (BNLMS) (20140121), Research Fund for the Doctoral Program of Higher Education of China (RFDP) (No. 20121101110049) and the 111 Project (B07012) for financial support.

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